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CLEAR + BRILLIANT PERMÉA™ - COFEPRIS Registration 203E2019 SSA

Access comprehensive regulatory information for CLEAR + BRILLIANT PERMÉA™ (CLEAR + BRILLIANT PERMÉA™) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 203E2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on February 06, 2019.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.

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COFEPRIS Official Data
Clase II
203E2019 SSA
CLEAR + BRILLIANT PERMÉA™
COFEPRIS Analysis ID: 203E2019 SSA
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Product Use / Uso del Producto
Spanish

EL SISTEMA LÁSER CLEAR + BRILLIANT ESTÁ DISEÑADO PARA PROCEDIMIENTOS DERMATOLÓGICOS QUE REQUIEREN LA COAGULACIÓN DE TEJIDOS BLANDOS Y PROCEDIMIENTOS GENERALES DE REJUVENECIMIENTO DE LA PIEL.

English

THE CLEAR + BRILLIANT LASER SYSTEM IS DESIGNED FOR DERMATOLOGICAL PROCEDURES REQUIRING SOFT TISSUE COAGULATION AND GENERAL SKIN REJUVENATION PROCEDURES.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
SISTEMA APLICADOR LASER
Trade Name (English)
LASER APPLICATOR SYSTEM
Registration Information
Analysis ID
203E2019 SSA
Registration Date
February 06, 2019
Manufacturer / Fabricante
Name (English)
BAUSCH & LOMB MÉXICO, S.A. DE C.V.